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Effectiveness of Drug Eluting TACE in Primary HCC

Primary Purpose

Hepatic Cell Carcinoma

Status
Unknown status
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
HepaSphere Microspheres/Doxorubicin Hydrochloride
Lipiodol
Sponsored by
Assiut University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatic Cell Carcinoma

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients must be 18 to 75 years old.
  • patients must be diagnosed as primary Hepatocellular carcinoma (HCC) by radiologic imaging revealed angiogenicity pattern .
  • All of the patient have Child-Pugh status A or B .
  • All of the patient have BCLC stage A or B.
  • patients must have adequate renal and liver function accepting the maneuver.
  • patients must have adequate coagulation profile (platelets count ≥ 80 000), (prothrombin concentration ≥ 70 %).
  • patients must haven't previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).

Exclusion Criteria:

  • patients have previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation).
  • patients with impaired coagulation profile (platelets count < 80 000), (prothrombin concentration < 70 %).
  • patients with decompensated liver cell failure having ascites which impedes the maneuver .
  • patients with past history of reaction to the drug used in maneuver
  • patients with poor image quality.
  • patients with lost follow up .

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    drug eluting bead trans arterial chemo embolization

    conventional trans arterial chemo embolization

    Arm Description

    the international arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Hepasphere

    the control arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Lipiodol

    Outcomes

    Primary Outcome Measures

    Evaluate the effectiveness of drug-eluting bead trans-arterial chemo-embolization in patients of hepatocellular carcinoma
    Evaluate the efficacy and safety of drug-eluting bead trans-arterial chemo-embolization in management of HCC patients in comparison of conventional chemo-embolization in 75 stable patients by evaluating the response of embolized lesions for each drug with modified RECIST criteria.

    Secondary Outcome Measures

    Full Information

    First Posted
    July 26, 2019
    Last Updated
    August 6, 2019
    Sponsor
    Assiut University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04048317
    Brief Title
    Effectiveness of Drug Eluting TACE in Primary HCC
    Official Title
    Effectiveness of Drug Eluting & Conventional Trans-arterial Chemo-embolization in Treatment of Primary Hepatic Cell Carcinoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 1, 2019 (Anticipated)
    Primary Completion Date
    September 1, 2020 (Anticipated)
    Study Completion Date
    December 1, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Assiut University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    the aim of this work to compare effectiveness of drug-eluting bead trans-arterial chemo-embolization and conventional trans-arterial chemo-embolization of hepatic cell carcinoma in the aspect of (Tumor response via m-RECIST criteria), (liver injury via Liver function tests and tumor markers) and (survival outcome) of patients treated in Assiut university .
    Detailed Description
    Hepatocellular carcinoma (HCC) is the sixth most common cancer in the world and the third most common cause of cancer-related death .. With improved surveillance of patients with chronic liver disease and advances in imaging, more patients are diagnosed with early-stage HCC . For the treatment of early stage HCC, curative therapies including liver transplantation, hepatic resection, and radio frequency ablation (RFA) are recommended. Liver transplantation is the treatment option especially for patients with decompensated cirrhosis, but potential recipients outnumber donors. Hepatic resection is widely used as the main choice of treatment for resectable HCC. However, the risk of postoperative hepatic dysfunction often precludes surgery. For unresectable patient, trans-arterial chemo-embolization (TACE) was the treatment of choice . At 2014, Yang et al. compared the treatment effects of hepatic resection, RFA, and conventional TACE on long-term survival. It was found that the range of patients treated by TACE in clinical practice reported survivals widely range from 8-26% at 5-years. which was similar to that with hepatic resection and RFA in patients with single-nodule HCC of 3 cm or smaller without vascular invasion when the underlying liver status was balanced among the patients receiving each treatment. In addition, most of the patients initially treated with c-TACE achieved a complete response, which was one of the independent prognostic factors of survival, although some should receive repeated treatments. However, when c-TACE is used as an initial treatment, special care should be taken to obtain a complete response, and surveillance for tumor recurrence should be undertaken. These results are consistent with those of cohort studies demonstrating that TACE provided overall survival similar to hepatic resection in early-stage HCC . Conventional (Lipiodol) TACE Base on technique with emulsified combination of chemotherapy such as Doxorubicin and Lipiodol administrate via arterial feeder. Less in systemic chemotherapy and increase overall survival rate were the most concern in treatment but many studies reported side effects from conventional (Lipiodol) TACE significantly among an improvement of overall survival rate . Conventional TACE may cause side effects because it can damage healthy cells as it kills cancer cells. Side effects can develop any time during, immediately after or a few days or weeks after chemotherapy . in addition to the patient needed frequent ablation after a short time . The most commonly Side Effect of TACE is (Post embolization syndrome) which is a group of symptoms . include : fever, Right upper quadrant pain, nausea, vomiting and fatigue . Other side effects may occur include bruising or bleeding at the catheter site, hair loss, abnormal liver functions, lung infections, gall bladder inflammation and tumor lysis syndrome . Drug-eluting bead TACE is the new method of delivering chemotherapy during TACE which uses special beads that already have the chemotherapy drug in them . after these are injected into the arteries of the liver , they slowly sustained releasing the drug to treat the tumor . The studies showed that TACE with (Hepasphere) less systemic side effect in patient than TACE with (Lipiodol) but no definite statistical difference in treatment and survival outcome. This study compares effectiveness of those methods in treatment of Hepatocellular carcinoma in Assiut university

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hepatic Cell Carcinoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    75 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    drug eluting bead trans arterial chemo embolization
    Arm Type
    Experimental
    Arm Description
    the international arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Hepasphere
    Arm Title
    conventional trans arterial chemo embolization
    Arm Type
    Placebo Comparator
    Arm Description
    the control arm is the patients embolized with drug eluting bead trans arterial chemo embolization using Lipiodol
    Intervention Type
    Drug
    Intervention Name(s)
    HepaSphere Microspheres/Doxorubicin Hydrochloride
    Intervention Description
    evaluation the tumor (size, location and pattern of enhancement) ;and ensure portal vein patency; then evaluation of hepatic arterial anatomy, after that we determine the tumor arterial feeders and the arteries that should be avoided during the maneuver. Selective celiac and superior mesenteric angiograms were performed using 5 Fr. Catheter then superselective angiogram were used microcatheter. then injection of drug-eluting microsphere (25 mg Hepasphere 50-100 micron) loaded with 50 mg doxorubicin solution for 2 hours.
    Intervention Type
    Drug
    Intervention Name(s)
    Lipiodol
    Intervention Description
    evaluation the tumor (size, location and pattern of enhancement) ;and ensure portal vein patency; then evaluation of hepatic arterial anatomy, after that we determine the tumor arterial feeders and the arteries that should be avoided during the maneuver. Selective celiac and superior mesenteric angiograms were performed using 5 Fr. Catheter then superselective angiogram were used microcatheter. then injection of prepared mixture of Lipiodol and (Doxorubicin or 5-FU) vary in dosage depend on operator consideration
    Primary Outcome Measure Information:
    Title
    Evaluate the effectiveness of drug-eluting bead trans-arterial chemo-embolization in patients of hepatocellular carcinoma
    Description
    Evaluate the efficacy and safety of drug-eluting bead trans-arterial chemo-embolization in management of HCC patients in comparison of conventional chemo-embolization in 75 stable patients by evaluating the response of embolized lesions for each drug with modified RECIST criteria.
    Time Frame
    baseline

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    75 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: patients must be 18 to 75 years old. patients must be diagnosed as primary Hepatocellular carcinoma (HCC) by radiologic imaging revealed angiogenicity pattern . All of the patient have Child-Pugh status A or B . All of the patient have BCLC stage A or B. patients must have adequate renal and liver function accepting the maneuver. patients must have adequate coagulation profile (platelets count ≥ 80 000), (prothrombin concentration ≥ 70 %). patients must haven't previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation). Exclusion Criteria: patients have previous history of resection of other ablation (alcohol, radio frequency or micro wave ablation). patients with impaired coagulation profile (platelets count < 80 000), (prothrombin concentration < 70 %). patients with decompensated liver cell failure having ascites which impedes the maneuver . patients with past history of reaction to the drug used in maneuver patients with poor image quality. patients with lost follow up .
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Ahmed M. Abdurabou, resident
    Phone
    00201149112036
    Email
    ahmedabdurabou@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Haisam A. Atta, professor
    Phone
    00201005017866
    Email
    haisamasa@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    Citations:
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    25220842
    Citation
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    Links:
    URL
    https://www.journalacs.org/article/S1072-7515(11)00896-9/abstract
    Description
    Hepatic Arterial Infusion of Doxorubicin-Loaded Microsphere for Treatment of Hepatocellular Cancer: A Multi-Institutional Registry

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